ES2163742T3 - Quinoxalinadionas. - Google Patents

Quinoxalinadionas.

Info

Publication number
ES2163742T3
ES2163742T3 ES97908156T ES97908156T ES2163742T3 ES 2163742 T3 ES2163742 T3 ES 2163742T3 ES 97908156 T ES97908156 T ES 97908156T ES 97908156 T ES97908156 T ES 97908156T ES 2163742 T3 ES2163742 T3 ES 2163742T3
Authority
ES
Spain
Prior art keywords
rent
ring
alcoxi
sub
arilo
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES97908156T
Other languages
English (en)
Inventor
David John Bull
Christopher Lee Carr
Michael Jonathan Fray
Elisabeth Colette Loui Gautier
Charles Eric Mowbray
Alan Stobie
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Research and Development Co NV SA
Original Assignee
Pfizer Research and Development Co NV SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Research and Development Co NV SA filed Critical Pfizer Research and Development Co NV SA
Application granted granted Critical
Publication of ES2163742T3 publication Critical patent/ES2163742T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Psychology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Luminescent Compositions (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Abstract

LA INVENCION PROPORCIONA COMPUESTOS DE FORMULA (I) Y LAS SALES FARMACEUTICAMENTE ACEPTABLES DE LOS MISMOS, EN LA QUE R ES UN GRUPO HETEROARILO CON UN ANILLO DE 5 ESLABONES QUE CONTIENEN 3 O 4 HETEROATOMOS DE NITROGENO, EL CUAL ESTA UNIDO AL ANILLO DE QUINOXALINDIONA MEDIANTE UN ATOMO DE CARBONO O DE NITROGENO DEL ANILLO, O ES UN GRUPO HETEROARILO CON UN ANILLO DE 6 ESLABONES QUE CONTIENEN ENTRE 1 Y 3 HETEROATOMOS DE NITROGENO QUE ESTA UNIDO AL ANILLO DE QUINOXALINDIONA MEDIANTE UN ATOMO DE CARBONO DEL ANILLO, ESTANDO DICHOS GRUPOS OPCIONALMENTE BENZO CONDENSADOS Y OPCIONALMENTE SUSTITUIDOS, INCLUYENDO EN LA PORCION BENZO CONDENSADA, MEDIANTE 1 O 2 SUSTITUYENTES, SELECCIONADO CADA UNO DE ELLOS INDEPENDIENTEMENTE ENTRE ALQUILO C SUB,1 -C 4 , ALQUENILO C 2 -C 4 , CICLOALQUILO C 3 -C 7 , HALOGENO, HIDROXI, ALCOXI C 1 -C 4 , OXICICLOALQUILO C 3 -C 7 , -COOH, ALCOXICARBONILO C 1 -C 4 , CONR 3 R 4 , -N 3 R 4 , -S(O) P(ALQUILO C 1 -C 4 ), -SO 2 NR 3 R 4 , ARI LO, OXIARILO, ARILALCOXI (C 1 -C 4 ) YHET, ESTANDO DICHO ALQUILO C 1 -C 4 OPCIONALMENTE SUSTITUIDO CON CIC LOALQUILO C 3 -C 7 , HALOGENO, HIDROXI, ALCOXI C 1-C 4 , HALOALCOXI (C 1 -C 4 ), OXICICLOALQUILO C SUB,3 C 7 , CICLOALQUIL C 3 -C 7 ALCOXI C 1 C4 ), -COOH, ALCOXI C 1 -C 4 CARBONILO, CONR 3 R 4 , -NR 3 R 4 , -S(O) P (ALQUILO C 1 -C 4 ), - SO 2 (ARILO), SO 2 NR 3 R 4 , MOR FOLINO, ARILO, OXIARILO, ARILALCOXI (C 1 -C 4 ) O HET, ESTANDO DICHO ALQUENILO C 2 -C 4 OPCIONALMENTE SUSTITUIDO CON ARILO; R 1 Y R 2 SE SELECCIONAN CADA UNO DE ELLOS INDEPENDIENTEMENTE ENTRE H, FLUORO, CLORO, BROMO, ALQUILO C 1 -C SUB.4 Y HALOALQUILO C 1 -C SUB.4 ; R 3 Y R 4 SE SELECCIONAN CADA UNO DE ELLOS INDEPENDIENTEMENTE ENTRE H Y ALQUILO C 1 C 4 O, CUANDO SE UNEN, SON ALQUI LENO C 5 -C 7 ; P ES 0, 1 O 2; JUNTO CON LA PREPARACION DE LAS COMPOSICIONES QUE LOS CONTIENEN, LOS USOS DE Y LOS INTERMEDIOS UTILIZADOS EN LA SINTESIS DE DICHOS COMPUESTOS. LOS COMPUESTOS SON UTILES COMO ANTAGONISTAS DEL RECEPTOR DE LA NMDA PARA EL TRATAMIENTO DE TRASTORNOS NEURODEGENERATIVOS AGUDOS Y NEUROLOGICOS CRONICOS.
ES97908156T 1996-03-09 1997-02-27 Quinoxalinadionas. Expired - Lifetime ES2163742T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9605027.3A GB9605027D0 (en) 1996-03-09 1996-03-09 Quinoxalinediones

Publications (1)

Publication Number Publication Date
ES2163742T3 true ES2163742T3 (es) 2002-02-01

Family

ID=10790134

Family Applications (1)

Application Number Title Priority Date Filing Date
ES97908156T Expired - Lifetime ES2163742T3 (es) 1996-03-09 1997-02-27 Quinoxalinadionas.

Country Status (42)

Country Link
US (1) US6376490B1 (es)
EP (1) EP0885212B1 (es)
JP (1) JP3110467B2 (es)
KR (1) KR100288099B1 (es)
CN (1) CN1103770C (es)
AP (1) AP767A (es)
AR (1) AR006119A1 (es)
AT (1) ATE208773T1 (es)
AU (1) AU717972B2 (es)
BG (1) BG63340B1 (es)
BR (1) BR9707851A (es)
CA (1) CA2248366C (es)
CO (1) CO4770976A1 (es)
CZ (1) CZ292792B6 (es)
DE (1) DE69708269T2 (es)
DK (1) DK0885212T3 (es)
DZ (1) DZ2188A1 (es)
EA (1) EA001730B1 (es)
ES (1) ES2163742T3 (es)
GB (1) GB9605027D0 (es)
HN (1) HN1998000034A (es)
HR (1) HRP970132A2 (es)
HU (1) HUP9900975A3 (es)
ID (1) ID18112A (es)
IL (1) IL125491A (es)
IS (1) IS4811A (es)
MA (1) MA26422A1 (es)
NO (1) NO984058L (es)
NZ (1) NZ331060A (es)
OA (1) OA10850A (es)
PE (2) PE43398A1 (es)
PL (1) PL329032A1 (es)
PT (1) PT885212E (es)
SI (1) SI0885212T1 (es)
SK (1) SK283467B6 (es)
TN (1) TNSN97044A1 (es)
TR (1) TR199801782T2 (es)
TW (1) TW454004B (es)
UY (1) UY24482A1 (es)
WO (1) WO1997032873A1 (es)
YU (2) YU39698A (es)
ZA (1) ZA971987B (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ336842A (en) * 1997-02-27 2000-05-26 Pfizer Process of making quinoxalinediones to produce antagonistic effect at NMDA receptors
AP982A (en) * 1997-02-27 2001-07-16 Pfizer Quinoxalinediones.
US6340758B1 (en) * 1997-05-16 2002-01-22 Warner-Lambert Company Conformationally semi-constrained quinoxaline 2,3-diones as neuroprotective agents
DE10005150A1 (de) * 2000-02-07 2001-08-09 Merck Patent Gmbh Verfahren zur Herstellung von 5-Arylnicotinaldehyden
CA2409819C (en) * 2000-05-19 2009-09-15 Yamanouchi Pharmaceutical Co., Ltd. Triazole derivatives
US7732162B2 (en) 2003-05-05 2010-06-08 Probiodrug Ag Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases
WO2005006945A2 (en) * 2003-07-03 2005-01-27 The Salk Institute For Biological Studies Methods for treating neural disorders and compounds useful therefor
MY145368A (en) 2004-01-13 2012-01-31 Nissan Chemical Ind Ltd Aminoquinoxaline compounds and polyaminoquinoxaline compounds, and use thereof
US7799894B2 (en) 2004-02-06 2010-09-21 Yamaguchi University Electrode for energy storage device and process for producing the same
JP2007223901A (ja) * 2004-03-24 2007-09-06 Takeda Chem Ind Ltd 複素環化合物およびその用途
US20060211739A1 (en) * 2005-02-08 2006-09-21 Arturo Perez-Medrano Use of selective P2X7 receptor antagonists
WO2007112347A1 (en) * 2006-03-28 2007-10-04 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
WO2008055945A1 (en) 2006-11-09 2008-05-15 Probiodrug Ag 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcer, cancer and other diseases
WO2008065141A1 (en) 2006-11-30 2008-06-05 Probiodrug Ag Novel inhibitors of glutaminyl cyclase
CA2686816A1 (en) 2007-01-16 2008-07-24 The Johns Hopkins University Use of various glutamate receptor antagonists for delaying or preventing platelet activity or for treating or preventing a thrombotic disease or disorder
EP2481408A3 (en) 2007-03-01 2013-01-09 Probiodrug AG New use of glutaminyl cyclase inhibitors
EP2865670B1 (en) 2007-04-18 2017-01-11 Probiodrug AG Thiourea derivatives as glutaminyl cyclase inhibitors
CN101679383B (zh) * 2007-05-17 2014-10-29 株式会社半导体能源研究所 三唑衍生物,和使用三唑衍生物的发光元件、发光器件和电子器件
US8486940B2 (en) 2009-09-11 2013-07-16 Probiodrug Ag Inhibitors
JP6026284B2 (ja) 2010-03-03 2016-11-16 プロビオドルグ エージー グルタミニルシクラーゼの阻害剤
EP2545047B9 (en) 2010-03-10 2015-06-10 Probiodrug AG Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5)
EP2560953B1 (en) 2010-04-21 2016-01-06 Probiodrug AG Inhibitors of glutaminyl cyclase
JP6050264B2 (ja) 2011-03-16 2016-12-21 プロビオドルグ エージー グルタミニルシクラーゼの阻害剤としてのベンゾイミダゾール誘導体
US9879004B2 (en) * 2013-02-07 2018-01-30 Merck Patent Gmbh Substituted acetylene derivatives and their use as positive allosteric modulators of mGluR4
PL3461819T3 (pl) 2017-09-29 2020-11-30 Probiodrug Ag Inhibitory cyklazy glutaminylowej
CN111548320B (zh) * 2019-10-09 2023-03-24 贵州大学 一类1,3,4-噁二唑酰肼类化合物及其制备方法和应用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69132340T2 (de) * 1990-11-06 2001-02-08 Yamanouchi Pharmaceutical Co., Ltd. Kondensiertes pyrazinderivat
DE4217952A1 (de) * 1992-05-30 1993-12-02 Basf Ag Chinoxalin-2,3(1H,4H)-dione
GB9418443D0 (en) 1994-09-13 1994-11-02 Pfizer Ltd Therapeutic agents
DE4439492A1 (de) * 1994-10-25 1996-05-02 Schering Ag Neue Chinoxalindionderivate, deren Herstellung und Verwendung in Arzneimitteln
NZ336842A (en) * 1997-02-27 2000-05-26 Pfizer Process of making quinoxalinediones to produce antagonistic effect at NMDA receptors

Also Published As

Publication number Publication date
TNSN97044A1 (fr) 2005-03-15
AR006119A1 (es) 1999-08-11
PL329032A1 (en) 1999-03-01
PE58199A1 (es) 1999-06-11
AU717972B2 (en) 2000-04-06
US6376490B1 (en) 2002-04-23
SK283467B6 (sk) 2003-08-05
NO984058D0 (no) 1998-09-03
AP767A (en) 1999-09-29
GB9605027D0 (en) 1996-05-08
EA199800702A1 (ru) 1999-04-29
KR19990087614A (ko) 1999-12-27
CN1103770C (zh) 2003-03-26
MA26422A1 (fr) 2004-12-20
DE69708269T2 (de) 2002-07-25
IL125491A0 (en) 1999-03-12
EA001730B1 (ru) 2001-08-27
ATE208773T1 (de) 2001-11-15
JPH11506123A (ja) 1999-06-02
CZ292792B6 (cs) 2003-12-17
UY24482A1 (es) 2000-09-29
TR199801782T2 (xx) 1998-12-21
DK0885212T3 (da) 2002-03-25
ID18112A (id) 1998-03-05
KR100288099B1 (ko) 2001-05-02
CA2248366C (en) 2002-06-04
CA2248366A1 (en) 1997-09-12
SK121498A3 (en) 2000-10-09
BG102760A (en) 1999-09-30
JP3110467B2 (ja) 2000-11-20
BR9707851A (pt) 1999-07-27
CZ286498A3 (cs) 1999-07-14
NO984058L (no) 1998-11-06
OA10850A (en) 2001-08-16
YU41199A (sh) 2001-09-28
HUP9900975A3 (en) 2001-12-28
WO1997032873A1 (en) 1997-09-12
HN1998000034A (es) 1999-02-09
CO4770976A1 (es) 1999-04-30
EP0885212A1 (en) 1998-12-23
PT885212E (pt) 2002-02-28
YU39698A (sh) 1999-03-04
IS4811A (is) 1998-07-27
DE69708269D1 (de) 2001-12-20
AP9700947A0 (en) 1997-04-30
AU2023197A (en) 1997-09-22
TW454004B (en) 2001-09-11
BG63340B1 (bg) 2001-10-31
ZA971987B (en) 1998-09-07
HRP970132A2 (en) 1998-06-30
IL125491A (en) 2003-07-06
HUP9900975A2 (hu) 1999-07-28
EP0885212B1 (en) 2001-11-14
CN1213369A (zh) 1999-04-07
NZ331060A (en) 2000-01-28
PE43398A1 (es) 1998-08-29
SI0885212T1 (en) 2002-02-28
DZ2188A1 (fr) 2002-12-02

Similar Documents

Publication Publication Date Title
ES2163742T3 (es) Quinoxalinadionas.
ES2151652T3 (es) Derivados de indol como antagonistas del receptor 5ht.
PA8550401A1 (es) Compuestos de heteroarilo biciclicos fusionados substituidos con heteroarilo como ligando del receptor gaba
ES2194205T3 (es) Derivados de triazolo-piridazina sustituidos como ligandos para los receptores gaba.
PE20081192A1 (es) Tratamiento del dolor
DK1379525T3 (da) Heteropolycykliske forbindelser og anvendelse deraf som metabotropiske glutamatreceptor-antagonister
ES2175350T3 (es) Compuestos triciclicos que tienen afinidad de union a receptores de melatonina, su produccion y uso.
UY27322A1 (es) Nuevos derivados de indol con afinidad por el receptor 5-ht6
ES2157366T3 (es) Derivados de pirimidindiona, pirimidintriona, triacindiona como antagonistas de receptores alfa-1-adrenergicos.
ES2158314T3 (es) Oximas, hidrazonas y olefinas sustituidas como antagonistas de la neuroquinina.
ES2194844T3 (es) Antagonistas del receptor de aminoacidos excitadores.
PA8547901A1 (es) Derivados de 4-piperacinilindol con afinidad receptora de 5-ht6
ECSP034640A (es) Derivados de feniletenilo o feniletinilo como antagonistas del receptor del glutamato
UY26874A1 (es) Compuestos heterocíclicos como ligandos de los receptores gaba
GT200500367A (es) Derivados novedosos pirrolidilo de compuestos heteroaromaticos
MX19448A (es) Procedimiento para la prreparacion de compuestos antagonistas de los receptores de aminoacidos excitadores; compuestos obtenidos y composicion farmaceutica que los incluye.
MX9303263A (es) Antagonistas de la angiotensina ii, procedimiento para su preparacion y formulaciones farmaceuticas que los contienen
UY30954A1 (es) Dihidro y tetrahidro oxazolopirimidinonas sustituidas, preparacion y uso de las mismas
ES2161231T3 (es) Compuestos heterociclicos como antagonistas de bradiquinina.
PE20080192A1 (es) PIRIDIN[3,4-b]PIRAZINONAS
DK0640592T3 (da) N-acylerede tricycliske azaheteroringe anvendelige som vasopressin-antagonister
GT200600165A (es) Derivados dihidrobenzofuranos y usos de los mismos
BRPI0516467A (pt) derivados indol 5-sulfonil-1-piperidinil substituìdos como antagonistas de receptor de 5-ht6 para o tratamento de distúrbios do snc
UY25300A1 (es) Composiciones conteniendo un antagonista alfa adrenérgico y un compuesto que eleva los niveles de cgmp para el tratamiento de la impotencia
ES2180041T3 (es) Derivados de 5-oxido de piridazino(4,5-b)quinoleina, su preparacion y su uso como antagonistas de glicina.

Legal Events

Date Code Title Description
FG2A Definitive protection

Ref document number: 885212

Country of ref document: ES